Disease Term Disease ID Gene Symbol Classification References Source
Hereditary sensory and autonomic neuropathy type 1 36386 SPTLC1 Causal Pathogenic evidence from ClinVar - ClinVar
ATL1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ATL3 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
SPTLC2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -